Completed

DRESSINgDACC Coated Post-operative Dressings for Surgical Site Infection Prevention in Vascular Surgery

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Study Aim

This study aims to evaluate if DACC coated post-operative dressings can prevent surgical site infections within 30 days after vascular surgery.

What is being tested

DACC-Coated Post Operative Dressing

Device
Who is being recruted

Surgical Wound+7

+ Bacterial Infections and Mycoses

+ Bacterial Infections

Over 18 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: January 2017
See protocol details

Summary

Principal SponsorHull University Teaching Hospitals NHS Trust
Last updated: January 31, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 19, 2017

Actual date on which the first participant was enrolled.

This study focuses on surgical site infections, which are infections that occur at the site of surgery and affect around 5% of people who undergo operations. The rate is even higher in vascular surgery, reaching up to 30%. The study aims to investigate the effectiveness and cost-effectiveness of a method to reduce these infection rates. The method involves using Leukomed Sorbact, a wound dressing coated with a chemical called Dialkylcarbamoylchloride (DACC). This chemical is derived from spider-silk and interacts with bacteria, causing them to be removed from the wound when the dressing is changed. The study targets adults undergoing vascular surgery, a population that is particularly at risk of surgical site infections. In this study, 718 patients from various centers across the UK will participate. They will be randomly assigned by computer to one of two groups. One group will have their wounds dressed with Leukomed Sorbact, while the other group will receive a standard dressing. The study will follow up with the patients 30 days after their operation to inspect their wounds for infection. Patients will also be asked to complete short questionnaires about their quality of life at this time and again at 3 months post-surgery. The main question the study aims to answer is whether a DACC-coated dressing applied after an operation reduces the risk of infection at the surgery site. The study will also explore whether this treatment is cost-effective and promotes satisfactory healing.

Official TitleA Randomised Controlled Trial to Assess the Clinical and Cost Effectiveness of Dialkylcarbamoylchloride (DACC) Coated Post-operative Dressings Versus Standard Care in the Prevention of Surgical Site Infection in Clean or Clean-contaminated, Vascular Surgery.
Principal SponsorHull University Teaching Hospitals NHS Trust
Last updated: January 31, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

722 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Surgical WoundBacterial Infections and MycosesBacterial InfectionsInfectionsPathologic ProcessesPostoperative ComplicationsSurgical Wound InfectionPathological Conditions, Signs and SymptomsWound InfectionWounds and Injuries

Criteria

2 inclusion criteria required to participate
Adults ≥18 yrs undergoing clean or clean-contaminated lower limb vascular surgery, with wounds closed by primary intention.

Able to understand the Patient Information Sheet and supplementary materials and capable and willing to give informed consent and follow the protocol requirements (including attending all follow-up visits and completing written questionnaires).

6 exclusion criteria prevent from participating
Patients on antibiotics for other conditions at the time of surgery or in the follow up period.

Patients undergoing any procedure that does not include lower limb incisions.

Allergies to any component of either the DACC-coated dressing or the control dressing.

Inability to give informed consent due to incapacity (as defined by the MCA 2005).

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
DACC-Coated Post-Operative Dressing

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Academic Vascular Surgery Unit, Vascular Laboratory, Alderson House, Hull Royal Infirmary

Hull, United KingdomOpen Academic Vascular Surgery Unit, Vascular Laboratory, Alderson House, Hull Royal Infirmary in Google Maps
CompletedOne Study Center